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FDA 510(k)

PORTABLE AIR PLETHYSMOGRAPH

K-Number: K895588 · 1990-03-27

ApplicantLife Sciences Manufacturing, Inc.
Decision Date1990-03-27
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PORTABLE AIR PLETHYSMOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Life Sciences Manufacturing, Inc.. It received FDA 510(k) clearance on 1990-03-27 under 510(k) number K895588. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTABLE AIR PLETHYSMOGRAPH?

PORTABLE AIR PLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1990-03-27. The listed applicant is Life Sciences Manufacturing, Inc.. The 510(k) number is K895588.

When did PORTABLE AIR PLETHYSMOGRAPH receive FDA 510(k) clearance?

PORTABLE AIR PLETHYSMOGRAPH received FDA 510(k) clearance on 1990-03-27, under 510(k) number K895588.

Who is the listed applicant for PORTABLE AIR PLETHYSMOGRAPH?

The FDA 510(k) record lists Life Sciences Manufacturing, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTABLE AIR PLETHYSMOGRAPH?

The FDA product code for PORTABLE AIR PLETHYSMOGRAPH is DSB.

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Other records listing Life Sciences Manufacturing, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K910905SFA-II MICROPROCESSOR-CONTROLLED MODULEK903700IPG-II MODULEK900365PAG MICROPROCESSOR-CONTROLLED MODULEK896500CWD/PPG MODULEK896528SFA MODULEK884624MVL/MODULAB WITH PVR MODULE

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Related Devices (Code: DSB)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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